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1,3-Propanediamine → N-(2-amino-4-fluorophenyl)-6-(3-aminopropylamino)nicotinamide

HRID 1695042
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인쇄 미리보기

반응식

HRID 1695042 반응식
[NH2:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[NH:9][C:10](=[O:18])[C:11]1[CH:16]=[CH:15][C:14](Cl)=[N:13][CH:12]=1.[CH2:19]([NH2:23])[CH2:20][CH2:21][NH2:22]>>[NH2:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[NH:9][C:10](=[O:18])[C:11]1[CH:16]=[CH:15][C:14]([NH:22][CH2:21][CH2:20][CH2:19][NH2:23])=[N:13][CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 4281,3-PropanediamineHCID 57993734N-(2-amino-4-fluorophenyl)-6-chloronicotinamide

생성물 1

HCID 57993745N-(2-amino-4-fluorophenyl)-6-(3-aminopropylamino)nicotinamide수율 52%

실험 절차

N-(2-amino-4-fluorophenyl)-6-chloronicotinamide (266 mg, 1 mmol) and 6 ml of 1,3-propanediamine were heated to 80° C. for 3 hours. The excess 1,3-propanediamine was removed under vacuum. To the residue was added 5 ml of 0.20 M NaOH. The mixture was extracted with 100 ml of ethyl acetate. The ethyl acetate was removed under vacuum to give the title compound (158 mg, 52% yield) as a brown solid. LC-MS (m/z) 304 (M+1).

후처리

  1. customThe excess 1,3-propanediamine was removed under vacuum
  2. additionTo the residue was added 5 ml of 0.20 M NaOH
  3. extraction
The mixture was extracted with 100 ml of ethyl acetate
  • customThe ethyl acetate was removed under vacuum
  • 출처 및 근거

    ORD 기록
    ord-36e25e93bba24dd6a4e16d7de5f56383
    출처 데이터셋
    uspto-grants-2012_04
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08158656B2

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